Insect resistance management with combinations of Cry1Be and Cry1F proteins

ABSTRACT

The subject invention relates in part to stacking Cry1Be toxins along with Cry1Fa toxins to prevent insects from developing resistance towards either toxin by itself. As discussed in more detail herein, the subject pair of proteins is a particularly advantageous combination, as no other pair of proteins is known to provide high levels of control and non-cross-resistant activity against both  Spodoptera frugiperda  (FAW) and  Ostrinia nubilalis  (ECB) insects. This dual, non-cross-resistant activity is also advantageous because it can reduce the number of proteins/genes needed to target these insects with multiple, non-cross-resistant proteins. This can reduce or eliminate the need for refuge acreage. Accordingly, the subject invention also relates generally to using four genes to provide three proteins for non-cross-resistant control of a first insect, and three proteins for non-cross-resistant control of a second insect. In preferred embodiments, the targeted insects are FAW and ECB.

CROSS-REFERENCE TO RELATED APPLICATIONS

This is a national phase application, filed pursuant to 35 U.S.C. §371, of PCT application No. PCT/US10/60808 filed on Dec. 16, 2010, which claims the benefit of U.S. provisional application No. 61/284,290, filed on Dec. 16, 2009. The prior applications are incorporated herein by reference in their entirety.

BACKGROUND

Humans grow corn for food and energy applications. Insects eat and damage corn plants and thereby undermine these human efforts.

Current in-plant transgenic control of these pests is achieved through plant expression of a crystal (Cry) delta endotoxin gene coding for the Cry1Fa protein from Bacillus thuringiensis. Cry1Fa is the protein toxin currently in the Herculex™ brand of Dow AgroSciences transgenic corn seeds (Herculex, Herculex-Extra, and Herculex-RW) that are resistant to fall armyworm (FAW, Spodoptera frugiperda) and European corn borer (ECB, Ostrinia nubilalis) insect pests. This protein works by binding to specific receptor(s) located in the midgut of insects, and forms pores within the gut cells. The formation of these pores prevents insects from regulating osmotic balance which results in their death.

However, some are concerned that insects might be able to develop resistance to the action of Cry1Fa through genetic alterations of the receptors within their gut that bind Cry1Fa. Insects that produce receptors with a reduced ability to bind Cry1Fa can be resistant to the activity of Cry1Fa, and thus survive on plants that express this protein.

With a single Cry toxin continuously present in the plant during growth conditions, there is concern that insects could develop resistance to the activity of this protein through genetic alterations of the receptor that binds Cry1Fa toxin in the insect gut. Reductions in toxin binding due to these alterations in the receptor would lead to reduced toxicity of the Cry1Fa possibly leading to eventual decreased effectiveness of the protein when expressed in a crop. See e.g. US 2009 0313717, which relates to a Cry2 protein plus a Vip3Aa, Cry1F, or Cry1A for control of Helicoverpa zea or armigera. WO 2009 132850 relates to Cry1F or Cry1A and Vip3Aa for controlling Spodoptera frugiperda. US 2008 0311096 relates to Cry1Ab for controlling Cry1F-resistant ECB.

Additional Cry toxins are listed at the website of the official B.t. nomenclature committee (Crickmore et al.; lifesci.sussex.ac.uk/home/Neil_Crickmore/Bt/). See Appendix A, attached. There are currently nearly 60 main groups of “Cry” toxins (Cry1-Cry59), with additional Cyt toxins and VIP toxins and the like. Many of each numeric group have capital-letter subgroups, and the capital letter subgroups have lower-cased letter sub-subgroups. (Cry1 has A-L, and Cry1A has a-i, for example).

The van Frankenhuyzen (2009) reference (J. Invert. Pathol. 101:1-16), for example, illustrates that there are many target pests and a great number of toxins that could potentially be selected to control the target pests. See e.g. FIG. 3 of van Frankenhuyzen. One (among many) pests that could be targeted would include Ostrinia nubilalis, and for this insect, FIG. 3 of van Frankenhuyzen shows 17 toxins that are active against ECB, and one that is possibly active. This is not an exhaustive list of the options.

FIG. 3 of van Frankenhuyzen also illustrates that each Cry protein has a unique spectrum of activity—they are active against some insects but not others. Cry proteins typically bind receptors on cells in the insect gut, and this is one factor that influences the spectrum of activity. Receptors for one Cry protein can be found in some insects but not in others; a given insect might have receptors for one or more Cry proteins but not for other Cry proteins.

Given many possible insects to target, and many possible Cry proteins that could be active against any given insect, numbers alone illustrate the complexity of the problem of resistance management. Considering just the 18 proteins identified by van Frankenhuyzen as active or possibly against ECB, this would allow for hundreds of possible pairs of toxins to test in combination.

In addition, assaying for competitive/non-competitive binding is no easy task. It can involve radio-active labeling and assaying for displacement of radioactively labeled proteins. This in and of itself can be a complex art.

Attempting to use resistant insects, directly, is also complicated. Resistant strains of insects would have to be developed against a given protein. Siqueira (June 2004; J. Econ. Entomol., 97(3):1049-1057) states (in the abstract) that “ . . . tests for cross-resistance among different toxins have been limited by a lack of resistant colonies.” This illustrates difficulties with obtaining resistant insect strains for assaying proteins for resistance management potential. When pairs of proteins are involved, either protein could be used in an attempt to screen for the development of resistant insects.

Siqueira also states, in the abstract, that selection with Cry1Ab (i.e., developing colonies of ECB that are resistant to Cry1Ab) “ . . . resulted in decreased susceptibility to a number of other toxins . . . . ” This illustrates the phenomenon of cross-resistance. Cry1Ab-resistant ECB were cross-resistant to “a number of other toxins.”

Thus, selecting two proteins that are active against the same (non-resistant) insect is a mere starting point of the analysis, if resistance issues are to be addressed. Activity levels against non-resistant insects is another factor. FIG. 11 of van Frankenhuyzen shows that even among a group of 12 toxins selected for testing against ECB (non-resistant), other Cry proteins (such as Cry1Ac, Cry1Bb, and Cry2Aa) could be more active than the ones now claimed for controlling ECB.

BRIEF SUMMARY

The subject invention relates in part to stacking Cry1Be proteins along with Cry1Fa proteins resulting in products that are more durable and less prone towards insects developing resistance towards either protein by itself.

As discussed in more detail herein, the subject pair of proteins is a particularly advantageous combination, as no other pair of proteins is known to provide high levels of control and non-cross-resistant action against both Spodoptera frugiperda (FAW) and Ostrinia nubilalis (ECB) insects.

This dual, non-cross-resistant activity is also advantageous because it can reduce the number of proteins/genes needed to target these insects with multiple, non-cross-resistant proteins. This can reduce or eliminate the need for refuge acreage. Accordingly, the subject invention also relates generally to using four genes to provide three proteins for non-cross-resistant control of FAW and three proteins for non-cross-resistant control of ECB.

DETAILED DESCRIPTION

The subject invention includes the use of Cry1Be proteins with Cry1Fa proteins as a pair. The subject invention also relates in part to triple stacks or “pyramids” of three (or more) toxins, with Cry1Fa and Cry1Be proteins being the base pair. The subject base pair of proteins provides two proteins providing non-cross-resistant action against two insects—the fall armyworm (FAW; Spodoptera frugiperda) and the European cornborer (ECB; Ostrinia nubilalis). This makes the subject pair of proteins a particularly advantageous combination, as no other pair of proteins is known to provide high levels of control and non-cross-resistant action against these two insects.

In some preferred pyramid embodiments, another protein can be added to the subject base pair to provide a third protein having action against ECB. Some of these preferred pyramid combinations are a Cry1Fa protein plus a Cry1Be protein plus another toxin/gene selected from the group consisting of Cry1Ab, Cry2Aa, Cry1I, and DIG-3 proteins.

In some preferred pyramid embodiments, another protein can be added to the subject base pair to provide a third protein having action against FAW. Some of these preferred pyramid combinations are Cry1Fa plus Cry1Be plus another toxin/gene selected from the group consisting of Vip3A, Cry1C, Cry1D, and Cry1E.

In some preferred embodiments, and in light of the activity of both Cry1F and Cry1Be against both ECB and FAW, the subject invention allows for the use of four proteins wherein three of the four proteins provide non-cross-resistant action against ECB, and three of the four proteins provide non-competitive action against FAW). Preferred quad stacks are Cry1Fa plus Cry1Be plus: Cry1C, Cry1D, Cry1E, or Vip3 (for targeting FAW), plus Cry1Ab, Cry2A, Cry1I, or DIG-3 (for targetting ECB).

Concurrently filed application entitled “Use of Vip3Ab for management of resistant insects” provides data showing that Vip3Ab is useful with Cry1F for managing insecticidal protein resistance in FAW, and that Vip3Ab and Cry1F do not competitively bind to FAW membrane preparations.

U.S. Ser. No. 61/284,281 (filed Dec. 16, 2009) shows that Cry1C is active against Cry1F-resistant FAW, and U.S. Ser. No. 61/284,252 (filed Dec. 16, 2009) shows that Cry1D is active against Cry1F-resistant FAW. These two applications also show that Cry1C does not compete with Cry1F for binding in FAW membrane preparations, and that Cry1D does not compete with Cry1F for binding in FAW membrane preparations.

U.S. Ser. No. 61/284,278 (filed Dec. 16, 2009) shows that Cry2A is active against Cry1F-resistant ECB.

Cry1Ab is disclosed in US 2008 0311096 as being useful for controlling Cry1F-resistant ECBs.

DIG-3 is disclosed in US 2010 0269223.

Vip3 toxins, for example, (including Vip3Ab in some preferred embodiments) are listed in the attached Appendix A. Cry proteins are also listed. Those GENBANK numbers can also be used to obtain the sequences for any of the genes and proteins disclosed or mentioned herein.

The subject invention also relates generally to the use of three insecticidal proteins (Cry proteins in some preferred embodiments) that do not cause cross-resistance with each other against a single target pest. The subject invention also relates generally to the use of four insecticidal proteins (Cry and Vip proteins in some preferred embodiments) that, in combination, provide high levels of control and non-cross-resistant activity against two target insects

Plants (and acreage planted with such plants) that produce combinations of the subject proteins are included within the scope of the subject invention. Additional toxins/genes can also be added, but preferred triple and quad (four-protein/gene) stacks would, according to the subject invention, advantageously and surprisingly provide three proteins with non-competitive action against FAW and/or ECB. This can help to reduce or eliminate the requirement for refuge acreage (e.g., less than 40%, less than 20%, less than 10%, less than 5%, or even 0% refuge). A field thus planted of over 10 acres is thus included within the subject invention.

The subject polynucleotide(s) are preferably in a genetic construct under control (operably linked/comprising) of a non-Bacillus-thuringiensis promoter. The subject polynucleotides can comprise codon usage for enhanced expression in a plant.

To counter act the ability of insects to develop resistance to Cry1Fa, we identified Cry toxins that non-competitively (with Cry1Fa) bind to protein receptors. Cry1Fa does not to displace Cry1Be binding to receptors located in the insect gut of FAW and ECB larvae. We found that Cry1Be Cry proteins that either interact with completely different receptors, or only partially overlap in their receptor interactions compared to Cry1Fa. The ability of these Cry1Be toxins to be toxic to FAW and ECB larvae, yet not fully interact with the same receptor sites as Cry1Fa, shows that their toxicity will not be affected by insects having developed genetic alterations of their Cry1Fa receptor as a mechanism to become resistant to the toxicity of Cry1Fa. Thus insects having developed resistance to Cry1Fa through a reduction in the ability of its gut receptors to bind Cry1Fa would still be susceptible to the toxicity of Cry1Be proteins which bind alternative receptor sites. We obtained biochemical data that supports this.

Having combinations of these proteins expressed in transgenic plants will thus be a useful and valuable mechanism to reduce the probability for the development of insect resistance in the field and thus lead towards a reduction in the requirement for refuge. These Cry1Be proteins have been studied for their activity against other major insect pests, both sensitive, and those resistant to Cry1Fa (rFAW and rECB), as shown in Table 1, Cry1Be is active against both resistant and susceptible ECB larvae. These data show the Cry1Be toxin interacting at separate target site(s) within the insect gut compared to Cry1Fa—thus making excellent stacking partners.

Stacking Cry1Fa expressing crops with one or more additional Cry genes, such as those expressing a Cry1Be protein toxins would result in an effective management strategy to prevent the ability of insects to develop tolerance to the activity of transgenic plants expressing these protein toxins. Since we show that the Cry1Be proteins interact at different sites compared to Cry1Fa, if resistance were to occur through alterations in the affinity of the insect gut receptors that bind to the Cry toxins, the alteration would have to occur in at least two different receptors simultaneously to allow the insects to survive on plants expressing the multiple proteins. The probability of this occurring is extremely remote, thus increasing the durability of the transgenic product to ward of insects being able to develop tolerance to the proteins.

We radio-iodinated trypsin truncated forms of Cry1Be protein toxins and used radioreceptor binding assay techniques to measure their binding interaction with putative receptor proteins located within the insect gut membranes. The gut membranes were prepared as brush border membrane vesicles (BBMV) by the method of Wolfersberger. Iodination of the toxins were conducted using either iodo beads or iodogen treated tubes from Pierce Chemicals. Specific activity of the radiolabeled toxin was approximately 1-4 μCi/μg protein. Binding studies were carried out essentially by the procedures of Liang.

Additional competitive binding data using labeled Cry1Fa is also presented below in the Examples section. These data also show non-cross-resistant activity of Cry1Fa and Cry1Be against both ECB and FAW.

The data presented herein shows that Cry1Be proteins interact at separate target site within the insect gut compared to Cry1Fa. Thus, these two proteins make excellent stacking partners.

Genes and toxins useful according to the subject invention include not only the full length sequences disclosed but also fragments of these sequences, variants, mutants, and fusion proteins which retain the characteristic pesticidal activity of the toxins specifically exemplified herein. As used herein, the terms “variants” or “variations” of genes refer to nucleotide sequences which encode the same toxins or which encode equivalent toxins having pesticidal activity. As used herein, the term “equivalent toxins” refers to toxins having the same or essentially the same biological activity against the target pests as the claimed toxins.

As used therein, the boundaries represent approximately 95% (Cry1Fa's and 1Be's), 78% (Cry1F's and Cry1B's), and 45% (Cry1's) sequence identity, per “Revision of the Nomenclature for the Bacillus thuringiensis Pesticidal Crystal Proteins,” N. Crickmore, D. R. Zeigler, J. Feitelson, E. Schnepf, J. Van Rie, D. Lereclus, J. Baum, and D. H. Dean. Microbiology and Molecular Biology Reviews (1998) Vol 62: 807-813. These cut offs can also be applied to the core proteins only (for Cry1Fa and Cry1Be core proteins, for example).

Fragments and equivalents that retain the pesticidal activity of the exemplified toxins would be within the scope of the subject invention. Also, because of the redundancy of the genetic code, a variety of different DNA sequences can encode the amino acid sequences disclosed herein. It is well within the skill of a person trained in the art to create these alternative DNA sequences encoding the same, or essentially the same, toxins. These variant DNA sequences are within the scope of the subject invention. As used herein, reference to “essentially the same” sequence refers to sequences which have amino acid substitutions, deletions, additions, or insertions which do not materially affect pesticidal activity. Fragments of genes encoding proteins that retain pesticidal activity are also included in this definition.

A further method for identifying the genes encoding the toxins and gene portions useful according to the subject invention is through the use of oligonucleotide probes. These probes are detectable nucleotide sequences. These sequences may be detectable by virtue of an appropriate label or may be made inherently fluorescent as described in International Application No. WO93/16094. As is well known in the art, if the probe molecule and nucleic acid sample hybridize by forming a strong bond between the two molecules, it can be reasonably assumed that the probe and sample have substantial homology. Preferably, hybridization is conducted under stringent conditions by techniques well-known in the art, as described, for example, in Keller, G. H., M. M. Manak (1987) DNA Probes, Stockton Press, New York, N.Y., pp. 169-170. Some examples of salt concentrations and temperature combinations are as follows (in order of increasing stringency): 2×SSPE or SSC at room temperature; 1×SSPE or SSC at 42° C.; 0.1×SSPE or SSC at 42° C.; 0.1×SSPE or SSC at 65° C. Detection of the probe provides a means for determining in a known manner whether hybridization has occurred. Such a probe analysis provides a rapid method for identifying toxin-encoding genes of the subject invention. The nucleotide segments which are used as probes according to the invention can be synthesized using a DNA synthesizer and standard procedures. These nucleotide sequences can also be used as PCR primers to amplify genes of the subject invention.

Certain proteins of the subject invention have been specifically exemplified herein. Since these proteins are merely exemplary of the proteins of the subject invention, it should be readily apparent that the subject invention comprises variant or equivalent proteins (and nucleotide sequences coding for equivalent proteins) having the same or similar pesticidal activity of the exemplified protein. Equivalent proteins will have amino acid homology with an exemplified protein. This amino acid homology will typically be greater than 75%, preferably be greater than 90%, and most preferably be greater than 95%. The amino acid homology will be highest in critical regions of the protein which account for biological activity or are involved in the determination of three-dimensional configuration which ultimately is responsible for the biological activity. In this regard, certain amino acid substitutions are acceptable and can be expected if these substitutions are in regions which are not critical to activity or are conservative amino acid substitutions which do not affect the three-dimensional configuration of the molecule. For example, amino acids may be placed in the following classes: non-polar, uncharged polar, basic, and acidic. Conservative substitutions whereby an amino acid of one class is replaced with another amino acid of the same type fall within the scope of the subject invention so long as the substitution does not materially alter the biological activity of the compound. Following is a listing of examples of amino acids belonging to each class. In some instances, non-conservative substitutions can also be made. The critical factor is that these substitutions must not significantly detract from the biological activity of the protein.

Class of Amino Acid Examples of Amino Acids Nonpolar Ala, Val, Leu, Ile, Pro, Met, Phe, Trp Uncharged Polar Gly, Ser, Thr, Cys, Tyr, Asn, Gln Acidic Asp, Glu Basic Lys, Arg, His

Plant Transformation.

A preferred recombinant host for production of the insecticidal proteins of the subject invention is a transformed plant. Genes encoding Bt toxin proteins, as disclosed herein, can be inserted into plant cells using a variety of techniques which are well known in the art. For example, a large number of cloning vectors comprising a replication system in Escherichia coli and a marker that permits selection of the transformed cells are available for preparation for the insertion of foreign genes into higher plants. The vectors comprise, for example, pBR322, pUC series, M13 mp series, pACYC184, inter alia. Accordingly, the DNA fragment having the sequence encoding the Bt toxin protein can be inserted into the vector at a suitable restriction site. The resulting plasmid is used for transformation into E. coli. The E. coli cells are cultivated in a suitable nutrient medium, then harvested and lysed. The plasmid is recovered. Sequence analysis, restriction analysis, electrophoresis, and other biochemical-molecular biological methods are generally carried out as methods of analysis. After each manipulation, the DNA sequence used can be cleaved and joined to the next DNA sequence. Each plasmid sequence can be cloned in the same or other plasmids. Depending on the method of inserting desired genes into the plant, other DNA sequences may be necessary. If, for example, the Ti or Ri plasmid is used for the transformation of the plant cell, then at least the right border, but often the right and the left border of the Ti or Ri plasmid T-DNA, has to be joined as the flanking region of the genes to be inserted. The use of T-DNA for the transformation of plant cells has been intensively researched and sufficiently described in EP 120 516, Lee and Gelvin (2008), Hoekema (1985), Fraley et al., (1986), and An et al., (1985), and is well established in the art.

Once the inserted DNA has been integrated in the plant genome, it is relatively stable. The transformation vector normally contains a selectable marker that confers on the transformed plant cells resistance to a biocide or an antibiotic, such as Bialaphos, Kanamycin, G418, Bleomycin, or Hygromycin, inter alia. The individually employed marker should accordingly permit the selection of transformed cells rather than cells that do not contain the inserted DNA.

A large number of techniques is available for inserting DNA into a plant host cell. Those techniques include transformation with T-DNA using Agrobacterium tumefaciens or Agrobacterium rhizogenes as transformation agent, fusion, injection, biolistics (microparticle bombardment), or electroporation as well as other possible methods. If Agrobacteria are used for the transformation, the DNA to be inserted has to be cloned into special plasmids, namely either into an intermediate vector or into a binary vector. The intermediate vectors can be integrated into the Ti or Ri plasmid by homologous recombination owing to sequences that are homologous to sequences in the T-DNA. The Ti or Ri plasmid also comprises the vir region necessary for the transfer of the T-DNA. Intermediate vectors cannot replicate themselves in Agrobacteria. The intermediate vector can be transferred into Agrobacterium tumefaciens by means of a helper plasmid (conjugation). Binary vectors can replicate themselves both in E. coli and in Agrobacteria. They comprise a selection marker gene and a linker or polylinker which are framed by the Right and Left T-DNA border regions. They can be transformed directly into Agrobacteria (Holsters et al., 1978). The Agrobacterium used as host cell is to comprise a plasmid carrying a vir region. The vir region is necessary for the transfer of the T-DNA into the plant cell. Additional T-DNA may be contained. The bacterium so transformed is used for the transformation of plant cells. Plant explants can advantageously be cultivated with Agrobacterium tumefaciens or Agrobacterium rhizogenes for the transfer of the DNA into the plant cell. Whole plants can then be regenerated from the infected plant material (for example, pieces of leaf, segments of stalk, roots, but also protoplasts or suspension-cultivated cells) in a suitable medium, which may contain antibiotics or biocides for selection. The plants so obtained can then be tested for the presence of the inserted DNA. No special demands are made of the plasmids in the case of injection and electroporation. It is possible to use ordinary plasmids, such as, for example, pUC derivatives.

The transformed cells grow inside the plants in the usual manner. They can form germ cells and transmit the transformed trait(s) to progeny plants. Such plants can be grown in the normal manner and crossed with plants that have the same transformed hereditary factors or other hereditary factors. The resulting hybrid individuals have the corresponding phenotypic properties.

In a preferred embodiment of the subject invention, plants will be transformed with genes wherein the codon usage has been optimized for plants. See, for example, U.S. Pat. No. 5,380,831, which is hereby incorporated by reference. While some truncated toxins are exemplified herein, it is well-known in the Bt art that 130 kDa-type (full-length) toxins have an N-terminal half that is the core toxin, and a C-terminal half that is the protoxin “tail.” Thus, appropriate “tails” can be used with truncated/core toxins of the subject invention. See e.g. U.S. Pat. No. 6,218,188 and U.S. Pat. No. 6,673,990. In addition, methods for creating synthetic Bt genes for use in plants are known in the art (Stewart and Burgin, 2007). One non-limiting example of a preferred transformed plant is a fertile maize plant comprising a plant expressible gene encoding a Cry1Fa protein, and further comprising a second plant expressible gene encoding a Cry1Ca protein.

Transfer (or introgression) of the Cry1Fa- and Cry1Ca-determined trait(s) into inbred maize lines can be achieved by recurrent selection breeding, for example by backcrossing. In this case, a desired recurrent parent is first crossed to a donor inbred (the non-recurrent parent) that carries the appropriate gene(s) for the Cry1F- and Cry1C-determined traits. The progeny of this cross is then mated back to the recurrent parent followed by selection in the resultant progeny for the desired trait(s) to be transferred from the non-recurrent parent. After three, preferably four, more preferably five or more generations of backcrosses with the recurrent parent with selection for the desired trait(s), the progeny will be heterozygous for loci controlling the trait(s) being transferred, but will be like the recurrent parent for most or almost all other genes (see, for example, Poehlman & Sleper (1995) Breeding Field Crops, 4th Ed., 172-175; Fehr (1987) Principles of Cultivar Development, Vol. 1: Theory and Technique, 360-376).

Insect Resistance Management (IRM) Strategies.

Roush et al., for example, outlines two-toxin strategies, also called “pyramiding” or “stacking,” for management of insecticidal transgenic crops. (The Royal Society. Phil. Trans. R. Soc. Lond. B. (1998) 353, 1777-1786).

On their website, the United States Environmental Protection Agency (epa.gov/oppbppd1/biopesticides/pips/bt_corn_refuge_2006.htm) publishes the following requirements for providing non-transgenic (i.e., non-B.t.) refuges (a section or block of non-Bt crops/corn) for use with transgenic crops producing a single Bt protein active against target pests.

-   -   “The specific structured requirements for corn borer-protected         Bt (Cry1Ab or Cry1F) corn products are as follows:     -   Structured refuges:         -   20% non-Lepidopteran Bt corn refuge in Corn Belt;         -   50% non-Lepidopteran Bt refuge in Cotton Belt     -   Blocks         -   Internal (i.e., within the Bt field)         -   External (i.e., separate fields within ½ mile (¼ mile if             possible) of the Bt field to maximize random mating)     -   In-field Strips         -   Strips must be at least 4 rows wide (preferably 6 rows) to             reduce the effects of larval movement”     -   In addition, the National Corn Growers Association, on their         website:         (ncga.com/insect-resistance-management-fact-sheet-bt-corn)         also provides similar guidance regarding the refuge         requirements. For example:     -   “Requirements of the Corn Borer IRM:     -   Plant at least 20% of your corn acres to refuge hybrids     -   In cotton producing regions, refuge must be 50%     -   Must be planted within ½ mile of the refuge hybrids     -   Refuge can be planted as strips within the Bt field; the refuge         strips must be at least 4 rows wide     -   Refuge may be treated with conventional pesticides only if         economic thresholds are reached for target insect     -   Bt-based sprayable insecticides cannot be used on the refuge         corn     -   Appropriate refuge must be planted on every farm with Bt corn”

As stated by Roush et al. (on pages 1780 and 1784 right column, for example), stacking or pyramiding of two different proteins each effective against the target pests and with little or no cross-resistance can allow for use of a smaller refuge. Roush suggests that for a successful stack, a refuge size of less than 10% refuge, can provide comparable resistance management to about 50% refuge for a single (non-pyramided) trait. For currently available pyramided Bt corn products, the U.S. Environmental Protection Agency requires significantly less (generally 5%) structured refuge of non-Bt corn be planted than for single trait products (generally 20%).

There are various ways of providing the IRM effects of a refuge, including various geometric planting patterns in the fields (as mentioned above) and in-bag seed mixtures, as discussed further by Roush et al. (supra), and U.S. Pat. No. 6,551,962.

The above percentages, or similar refuge ratios, can be used for the subject double or triple stacks or pyramids. For triple stacks with three modes of action against a single target pest, a goal would be zero refuge (or less than 5% refuge, for example). This is particularly true for commercial acreage—of over 10 acres for example.

All patents, patent applications, provisional applications, and publications referred to or cited herein are incorporated by reference in their entirety to the extent they are not inconsistent with the explicit teachings of this specification. Unless specifically indicated or implied, the terms “a”, “an”, and “the” signify “at least one” as used herein.

REFERENCES

-   Wolfersberger, M. G., (1993), Preparation and Partial     Characterization of Amino Acid Transporting Brush Border Membrane     Vesicles from the Larval Midgut of the Gypsy Moth (Lymantria     Dispar). Arch. Insect Biochem. Physiol. 24: 139-147. -   Liang, Y., Patel, S. S., and Dean, D. H., (1995), Irreversible     Binding Kinetics of Bacillus thuringiensis Cry1A Delta-Endotoxins to     Gypsy Moth Brush Border Membrane Vesicles is Directly Correlated to     Toxicity. J. Biol. Chem., 270, 24719-24724.

EXAMPLES Example 1 Bioactivity

Bioassay results of the subject Cry proteins acting on FAW, ECB, and Cry1Fa resistant FAW and ECB insects are shown in Table 1. Both proteins are highly active against FAW larvae. (For a discussion of this pest, see e.g. Tabashnik, PNAS (2008), vol. 105 no. 49, 19029-19030.) Cry1Fa is much less active against FAW that are resistant towards the toxicity of Cry1Fa (rFAW) as compare to sensitive FAW. Cry1Be is as active, or more active, against rFAW as compared to sensitive FAW.

TABLE 1 Table 1. Biological activity of Cry proteins against four different insect types, plus Cry1Fa resistant FAW and ECB larvae. Non-underlined values in green are LC-50 values expressed as ranges of values obtained from multiple determinations. Underlined values are GI-50 values where the protein does not result in lethality against the particular insect. Values are in ng/cm². PRO- TEIN CEW FAW rFAW ECB rECB BCW Cry1Be 400-1,000 1,000-2,000 300 600 200-1,200 2,000 Cry1Fa 40-120  20-80 in- 20-100 inactive   200 active

Example 2 Binding Studies

FIG. 1 shows competition binding of ¹²⁵I Cry1Fa versus Cry1Fa or Cry1Be to brush border membrane vesicles produced from Spodoptera frugiperda (fall armyworm, FAW). Assays were conducted in duplicate using the pull-down method. FAW-0 represents ¹²⁵I Cry1Fa bound to receptors in the absence of any competing ligand (control). FAW-1,000 nM Cry1Fa represents the greatly reduced level of binding obtained in the presence of homologous non-labeled Cry1Fa which displaced the binding of the radiolabeled Cry1Fa from its receptor. FAW-1,000 nM Cry1Be represents the binding obtained in the presence of non-labeled Cry1Be which could not displace the binding of the radiolabeled Cry1Fa from its receptor.

FIG. 2 shows competition binding of ¹²⁵I Cry1Fa versus Cry1Fa or Cry1Be to brush border membrane vesicles produced from Ostrinia nubilalis (European corn borer, ECB). Assays were conducted in duplicate using the pull-down method. “Control Rxn” represents ¹²⁵I Cry1Fa bound to receptors in the absence of any competing ligand. 1,000 nM Cry1Fa represents the greatly reduced level of binding obtained in the presence of homologous non-labeled Cry1Fa which displaced the binding of the radiolabeled Cry1Fa from its receptor. 1,000 nM Cry1Be represents the binding obtained in the presence of non-labeled Cry1Be which could not displace the binding of the radiolabeled Cry1Fa from its receptor.

FIG. 3 shows competitive displacement of ¹²⁵I Cry1Be binding to brush border membrane vesicles produced from Spodoptera frugiperda by Cry1Fa (▴) and Cry1Be (●). Cry1Fa effectively displaces the binding of 0.5 nM ¹²⁵I Cry1Be only at concentrations greater than 100 nM (200-times the concentration of radiolabeled Cry1Be used in the assay). Cry1Be is much more effective at displacing itself as compared to Cry1Fa, even though Cry1Fa is more active against this pest than Cry1Be.

APPENDIX A List of delta-endotoxins—from Crickmore et al. website (cited in application) Accession Number is to NCBI entry (if available) Name Acc No. Authors Year Source Strain Comment Cry1Aa1 AAA22353 Schnepf et al 1985 Bt kurstaki HD1 Cry1Aa2 AAA22552 Shibano et al 1985 Bt sotto Cry1Aa3 BAA00257 Shimizu et al 1988 Bt aizawai IPL7 Cry1Aa4 CAA31886 Masson et al 1989 Bt entomocidus Cry1Aa5 BAA04468 Udayasuriyan et al 1994 Bt Fu-2-7 Cry1Aa6 AAA86265 Masson et al 1994 Bt kurstaki NRD-12 Cry1Aa7 AAD46139 Osman et al 1999 Bt C12 Cry1Aa8 I26149 Liu 1996 DNA sequence only Cry1Aa9 BAA77213 Nagamatsu et al 1999 Bt dendrolimus T84A1 Cry1Aa10 AAD55382 Hou and Chen 1999 Bt kurstaki HD-1-02 Cry1Aa11 CAA70856 Tounsi et al 1999 Bt kurstaki Cry1Aa12 AAP80146 Yao et al 2001 Bt Ly30 Cry1Aa13 AAM44305 Zhong et al 2002 Bt sotto Cry1Aa14 AAP40639 Ren et al 2002 unpublished Cry1Aa15 AAY66993 Sauka et al 2005 Bt INTA Mol-12 Cry1Ab1 AAA22330 Wabiko et al 1986 Bt berliner 1715 Cry1Ab2 AAA22613 Thorne et al 1986 Bt kurstaki Cry1Ab3 AAA22561 Geiser et al 1986 Bt kurstaki HD1 Cry1Ab4 BAA00071 Kondo et al 1987 Bt kurstaki HD1 Cry1Ab5 CAA28405 Hofte et al 1986 Bt berliner 1715 Cry1Ab6 AAA22420 Hefford et al 1987 Bt kurstaki NRD-12 Cry1Ab7 CAA31620 Haider & Ellar 1988 Bt aizawai IC1 Cry1Ab8 AAA22551 Oeda et al 1987 Bt aizawai IPL7 Cry1Ab9 CAA38701 Chak & Jen 1993 Bt aizawai HD133 Cry1Ab10 A29125 Fischhoff et al 1987 Bt kurstaki HD1 Cry1Ab11 I12419 Ely & Tippett 1995 Bt A20 DNA sequence only Cry1Ab12 AAC64003 Silva-Werneck et al 1998 Bt kurstaki S93 Cry1Ab13 AAN76494 Tan et al 2002 Bt c005 Cry1Ab14 AAG16877 Meza-Basso & Theoduloz 2000 Native Chilean Bt Cry1Ab15 AAO13302 Li et al 2001 Bt B-Hm-16 Cry1Ab16 AAK55546 Yu et al 2002 Bt AC-11 Cry1Ab17 AAT46415 Huang et al 2004 Bt WB9 Cry1Ab18 AAQ88259 Stobdan et al 2004 Bt Cry1Ab19 AAW31761 Zhong et al 2005 Bt X-2 Cry1Ab20 ABB72460 Liu et al 2006 BtC008 Cry1Ab21 ABS18384 Swiecicka et al 2007 Bt IS5056 Cry1Ab22 ABW87320 Wu and Feng 2008 BtS2491Ab Cry1Ab-like AAK14336 Nagarathinam et al 2001 Bt kunthala RX24 uncertain sequence Cry1Ab-like AAK14337 Nagarathinam et al 2001 Bt kunthala RX28 uncertain sequence Cry1Ab-like AAK14338 Nagarathinam et al 2001 Bt kunthala RX27 uncertain sequence Cry1Ab-like ABG88858 Lin et al 2006 Bt ly4a3 insufficient sequence Cry1Ac1 AAA22331 Adang et al 1985 Bt kurstaki HD73 Cry1Ac2 AAA22338 Von Tersch et al 1991 Bt kenyae Cry1Ac3 CAA38098 Dardenne et al 1990 Bt BTS89A Cry1Ac4 AAA73077 Feitelson 1991 Bt kurstaki PS85A1 Cry1Ac5 AAA22339 Feitelson 1992 Bt kurstaki PS81GG Cry1Ac6 AAA86266 Masson et al 1994 Bt kurstaki NRD-12 Cry1Ac7 AAB46989 Herrera et al 1994 Bt kurstaki HD73 Cry1Ac8 AAC44841 Omolo et al 1997 Bt kurstaki HD73 Cry1Ac9 AAB49768 Gleave et al 1992 Bt DSIR732 Cry1Ac10 CAA05505 Sun 1997 Bt kurstaki YBT-1520 Cry1Ac11 CAA10270 Makhdoom & Riazuddin 1998 Cry1Ac12 I12418 Ely & Tippett 1995 Bt A20 DNA sequence only Cry1Ac13 AAD38701 Qiao et al 1999 Bt kurstaki HD1 Cry1Ac14 AAQ06607 Yao et al 2002 Bt Ly30 Cry1Ac15 AAN07788 Tzeng et al 2001 Bt from Taiwan Cry1Ac16 AAU87037 Zhao et al 2005 Bt H3 Cry1Ac17 AAX18704 Hire et al 2005 Bt kenyae HD549 Cry1Ac18 AAY88347 Kaur & Allam 2005 Bt SK-729 Cry1Ac19 ABD37053 Gao et al 2005 Bt C-33 Cry1Ac20 ABB89046 Tan et al 2005 Cry1Ac21 AAY66992 Sauka et al 2005 INTA Mol-12 Cry1Ac22 ABZ01836 Zhang & Fang 2008 Bt W015-1 Cry1Ac23 CAQ30431 Kashyap et al 2008 Bt Cry1Ac24 ABL01535 Arango et al 2008 Bt 146-158-01 Cry1Ac25 FJ513324 Guan Peng et al 2008 Bt Tm37-6 No NCBI link July 2009 Cry1Ac26 FJ617446 Guan Peng et al 2009 Bt Tm41-4 No NCBI link July 2009 Cry1Ac27 FJ617447 Guan Peng et al 2009 Bt Tm44-1B No NCBI link July 2009 Cry1Ac28 ACM90319 Li et al 2009 Bt Q-12 Cry1Ad1 AAA22340 Feitelson 1993 Bt aizawai PS81I Cry1Ad2 CAA01880 Anonymous 1995 Bt PS81RR1 Cry1Ae1 AAA22410 Lee & Aronson 1991 Bt alesti Cry1Af1 AAB82749 Kang et al 1997 Bt NT0423 Cry1Ag1 AAD46137 Mustafa 1999 Cry1Ah1 AAQ14326 Tan et al 2000 Cry1Ah2 ABB76664 Qi et al 2005 Bt alesti Cry1Ai1 AAO39719 Wang et al 2002 Cry1A-like AAK14339 Nagarathinam et al 2001 Bt kunthala nags3 uncertain sequence Cry1Ba1 CAA29898 Brizzard & Whiteley 1988 Bt thuringiensis HD2 Cry1Ba2 CAA65003 Soetaert 1996 Bt entomocidus HD110 Cry1Ba3 AAK63251 Zhang et al 2001 Cry1Ba4 AAK51084 Nathan et al 2001 Bt entomocidus HD9 Cry1Ba5 ABO20894 Song et al 2007 Bt sfw-12 Cry1Ba6 ABL60921 Martins et al 2006 Bt S601 Cry1Bb1 AAA22344 Donovan et al 1994 Bt EG5847 Cry1Bc1 CAA86568 Bishop et al 1994 Bt morrisoni Cry1Bd1 AAD10292 Kuo et al 2000 Bt wuhanensis HD525 Cry1Bd2 AAM93496 Isakova et al 2002 Bt 834 Cry1Be1 AAC32850 Payne et al 1998 Bt PS158C2 Cry1Be2 AAQ52387 Baum et al 2003 Cry1Be3 FJ716102 Xiaodong Sun et al 2009 Bt No NCBI link July 2009 Cry1Bf1 CAC50778 Arnaut et al 2001 Cry1Bf2 AAQ52380 Baum et al 2003 Cry1Bg1 AAO39720 Wang et al 2002 Cry1Ca1 CAA30396 Honee et al 1988 Bt entomocidus 60.5 Cry1Ca2 CAA31951 Sanchis et al 1989 Bt aizawai 7.29 Cry1Ca3 AAA22343 Feitelson 1993 Bt aizawai PS81I Cry1Ca4 CAA01886 Van Mellaert et al 1990 Bt entomocidus HD110 Cry1Ca5 CAA65457 Strizhov 1996 Bt aizawai 7.29 Cry1Ca6 AAF37224 Yu et al 2000 Bt AF-2 Cry1Ca7 AAG50438 Aixing et al 2000 Bt J8 Cry1Ca8 AAM00264 Chen et al 2001 Bt c002 Cry1Ca9 AAL79362 Kao et al 2003 Bt G10-01A Cry1Ca10 AAN16462 Lin et al 2003 Bt E05-20a Cry1Ca11 AAX53094 Cai et al 2005 Bt C-33 Cry1Cb1 M97880 Kalman et al 1993 Bt galleriae HD29 DNA sequence only Cry1Cb2 AAG35409 Song et al 2000 Bt c001 Cry1Cb3 ACD50894 Huang et al 2008 Bt 087 Cry1Cb-like AAX63901 Thammasittirong et al 2005 Bt TA476-1 insufficient sequence Cry1Da1 CAA38099 Hofte et al 1990 Bt aizawai HD68 Cry1Da2 I76415 Payne & Sick 1997 DNA sequence only Cry1Db1 CAA80234 Lambert 1993 Bt BTS00349A Cry1Db2 AAK48937 Li et al 2001 Bt B-Pr-88 Cry1Dc1 ABK35074 Lertwiriyawong et al 2006 Bt JC291 Cry1Ea1 CAA37933 Visser et al 1990 Bt kenyae 4F1 Cry1Ea2 CAA39609 Bosse et al 1990 Bt kenyae Cry1Ea3 AAA22345 Feitelson 1991 Bt kenyae PS81F Cry1Ea4 AAD04732 Barboza-Corona et al 1998 Bt kenyae LBIT-147 Cry1Ea5 A15535 Botterman et al 1994 DNA sequence only Cry1Ea6 AAL50330 Sun et al 1999 Bt YBT-032 Cry1Ea7 AAW72936 Huehne et al 2005 Bt JC190 Cry1Ea8 ABX11258 Huang et al 2007 Bt HZM2 Cry1Eb1 AAA22346 Feitelson 1993 Bt aizawai PS81A2 Cry1Fa1 AAA22348 Chambers et al 1991 Bt aizawai EG6346 Cry1Fa2 AAA22347 Feitelson 1993 Bt aizawai PS81I Cry1Fb1 CAA80235 Lambert 1993 Bt BTS00349A Cry1Fb2 BAA25298 Masuda & Asano 1998 Bt morrisoni INA67 Cry1Fb3 AAF21767 Song et al 1998 Bt morrisoni Cry1Fb4 AAC10641 Payne et al 1997 Cry1Fb5 AAO13295 Li et al 2001 Bt B-Pr-88 Cry1Fb6 ACD50892 Huang et al 2008 Bt 012 Cry1Fb7 ACD50893 Huang et al 2008 Bt 087 Cry1Ga1 CAA80233 Lambert 1993 Bt BTS0349A Cry1Ga2 CAA70506 Shevelev et al 1997 Bt wuhanensis Cry1Gb1 AAD10291 Kuo & Chak 1999 Bt wuhanensis HD525 Cry1Gb2 AAO13756 Li et al 2000 Bt B-Pr-88 Cry1Gc AAQ52381 Baum et al 2003 Cry1Ha1 CAA80236 Lambert 1993 Bt BTS02069AA Cry1Hb1 AAA79694 Koo et al 1995 Bt morrisoni BF190 Cry1H-like AAF01213 Srifah et al 1999 Bt JC291 insufficient sequence Cry1Ia1 CAA44633 Tailor et al 1992 Bt kurstaki Cry1Ia2 AAA22354 Gleave et al 1993 Bt kurstaki Cry1Ia3 AAC36999 Shin et al 1995 Bt kurstaki HD1 Cry1Ia4 AAB00958 Kostichka et al 1996 Bt AB88 Cry1Ia5 CAA70124 Selvapandiyan 1996 Bt 61 Cry1Ia6 AAC26910 Zhong et al 1998 Bt kurstaki S101 Cry1Ia7 AAM73516 Porcar et al 2000 Bt Cry1Ia8 AAK66742 Song et al 2001 Cry1Ia9 AAQ08616 Yao et al 2002 Bt Ly30 Cry1Ia10 AAP86782 Espindola et al 2003 Bt thuringiensis Cry1Ia11 CAC85964 Tounsi et al 2003 Bt kurstaki BNS3 Cry1Ia12 AAV53390 Grossi de Sa et al 2005 Bt Cry1Ia13 ABF83202 Martins et al 2006 Bt Cry1Ia14 ACG63871 Liu & Guo 2008 Bt11 Cry1Ia15 FJ617445 Guan Peng et al 2009 Bt E-1B No NCBI link July 2009 Cry1Ia16 FJ617448 Guan Peng et al 2009 Bt E-1A No NCBI link July 2009 Cry1Ib1 AAA82114 Shin et al 1995 Bt entomocidus BP465 Cry1Ib2 ABW88019 Guan et al 2007 Bt PP61 Cry1Ib3 ACD75515 Liu & Guo 2008 Bt GS8 Cry1Ic1 AAC62933 Osman et al 1998 Bt C18 Cry1Ic2 AAE71691 Osman et al 2001 Cry1Id1 AAD44366 Choi 2000 Cry1Ie1 AAG43526 Song et al 2000 Bt BTC007 Cry1If1 AAQ52382 Baum et al 2003 Cry1I-like AAC31094 Payne et al 1998 insufficient sequence Cry1I-like ABG88859 Lin & Fang 2006 Bt ly4a3 insufficient sequence Cry1Ja1 AAA22341 Donovan 1994 Bt EG5847 Cry1Jb1 AAA98959 Von Tersch & Gonzalez 1994 Bt EG5092 Cry1Jc1 AAC31092 Payne et al 1998 Cry1Jc2 AAQ52372 Baum et al 2003 Cry1Jd1 CAC50779 Arnaut et al 2001 Bt Cry1Ka1 AAB00376 Koo et al 1995 Bt morrisoni BF190 Cry1La1 AAS60191 Je et al 2004 Bt kurstaki K1 Cry1-like AAC31091 Payne et al 1998 insufficient sequence Cry2Aa1 AAA22335 Donovan et al 1989 Bt kurstaki Cry2Aa2 AAA83516 Widner & Whiteley 1989 Bt kurstaki HD1 Cry2Aa3 D86064 Sasaki et al 1997 Bt sotto DNA sequence only Cry2Aa4 AAC04867 Misra et al 1998 Bt kenyae HD549 Cry2Aa5 CAA10671 Yu & Pang 1999 Bt SL39 Cry2Aa6 CAA10672 Yu & Pang 1999 Bt YZ71 Cry2Aa7 CAA10670 Yu & Pang 1999 Bt CY29 Cry2Aa8 AAO13734 Wei et al 2000 Bt Dongbei 66 Cry2Aa9 AAO13750 Zhang et al 2000 Cry2Aa10 AAQ04263 Yao et al 2001 Cry2Aa11 AAQ52384 Baum et al 2003 Cry2Aa12 ABI83671 Tan et al 2006 Bt Rpp39 Cry2Aa13 ABL01536 Arango et al 2008 Bt 146-158-01 Cry2Aa14 ACF04939 Hire et al 2008 Bt HD-550 Cry2Ab1 AAA22342 Widner & Whiteley 1989 Bt kurstaki HD1 Cry2Ab2 CAA39075 Dankocsik et al 1990 Bt kurstaki HD1 Cry2Ab3 AAG36762 Chen et al 1999 Bt BTC002 Cry2Ab4 AAO13296 Li et al 2001 Bt B-Pr-88 Cry2Ab5 AAQ04609 Yao et al 2001 Bt ly30 Cry2Ab6 AAP59457 Wang et al 2003 Bt WZ-7 Cry2Ab7 AAZ66347 Udayasuriyan et al 2005 Bt 14-1 Cry2Ab8 ABC95996 Huang et al 2006 Bt WB2 Cry2Ab9 ABC74968 Zhang et al 2005 Bt LLB6 Cry2Ab10 EF157306 Lin et al 2006 Bt LyD Cry2Ab11 CAM84575 Saleem et al 2007 Bt CMBL-BT1 Cry2Ab12 ABM21764 Lin et al 2007 Bt LyD Cry2Ab13 ACG76120 Zhu et al 2008 Bt ywc5-4 Cry2Ab14 ACG76121 Zhu et al 2008 Bt Bts Cry2Ac1 CAA40536 Aronson 1991 Bt shanghai S1 Cry2Ac2 AAG35410 Song et al 2000 Cry2Ac3 AAQ52385 Baum et al 2003 Cry2Ac4 ABC95997 Huang et al 2006 Bt WB9 Cry2Ac5 ABC74969 Zhang et al 2005 Cry2Ac6 ABC74793 Xia et al 2006 Bt wuhanensis Cry2Ac7 CAL18690 Saleem et al 2008 Bt SBSBT-1 Cry2Ac8 CAM09325 Saleem et al 2007 Bt CMBL-BT1 Cry2Ac9 CAM09326 Saleem et al 2007 Bt CMBL-BT2 Cry2Ac10 ABN15104 Bai et al 2007 Bt QCL-1 Cry2Ac11 CAM83895 Saleem et al 2007 Bt HD29 Cry2Ac12 CAM83896 Saleem et al 2007 Bt CMBL-BT3 Cry2Ad1 AAF09583 Choi et al 1999 Bt BR30 Cry2Ad2 ABC86927 Huang et al 2006 Bt WB10 Cry2Ad3 CAK29504 Saleem et al 2006 Bt 5_2AcT(1) Cry2Ad4 CAM32331 Saleem et al 2007 Bt CMBL-BT2 Cry2Ad5 CAO78739 Saleem et al 2007 Bt HD29 Cry2Ae1 AAQ52362 Baum et al 2003 Cry2Af1 ABO30519 Beard et al 2007 Bt C81 Cry2Ag ACH91610 Zhu et al 2008 Bt JF19-2 Cry2Ah EU939453 Zhang et al 2008 Bt No NCBI link July 2009 Cry2Ah2 ACL80665 Zhang et al 2009 Bt BRC-ZQL3 Cry2Ai FJ788388 Udayasuriyan et al 2009 Bt No NCBI link July 2009 Cry3Aa1 AAA22336 Herrnstadt et al 1987 Bt san diego Cry3Aa2 AAA22541 Sekar et al 1987 Bt tenebrionis Cry3Aa3 CAA68482 Hofte et al 1987 Cry3Aa4 AAA22542 McPherson et al 1988 Bt tenebrionis Cry3Aa5 AAA50255 Donovan et al 1988 Bt morrisoni EG2158 Cry3Aa6 AAC43266 Adams et al 1994 Bt tenebrionis Cry3Aa7 CAB41411 Zhang et al 1999 Bt 22 Cry3Aa8 AAS79487 Gao and Cai 2004 Bt YM-03 Cry3Aa9 AAW05659 Bulla and Candas 2004 Bt UTD-001 Cry3Aa10 AAU29411 Chen et al 2004 Bt 886 Cry3Aa11 AAW82872 Kurt et al 2005 Bt tenebrionis Mm2 Cry3Aa12 ABY49136 Sezen et al 2008 Bt tenebrionis Cry3Ba1 CAA34983 Sick et al 1990 Bt tolworthi 43F Cry3Ba2 CAA00645 Peferoen et al 1990 Bt PGSI208 Cry3Bb1 AAA22334 Donovan et al 1992 Bt EG4961 Cry3Bb2 AAA74198 Donovan et al 1995 Bt EG5144 Cry3Bb3 I15475 Peferoen et al 1995 DNA sequence only Cry3Ca1 CAA42469 Lambert et al 1992 Bt kurstaki BtI109P Cry4Aa1 CAA68485 Ward & Ellar 1987 Bt israelensis Cry4Aa2 BAA00179 Sen et al 1988 Bt israelensis HD522 Cry4Aa3 CAD30148 Berry et al 2002 Bt israelensis Cry4A-like AAY96321 Mahalakshmi et al 2005 Bt LDC-9 insufficient sequence Cry4Ba1 CAA30312 Chungjatpornchai et al 1988 Bt israelensis 4Q2-72 Cry4Ba2 CAA30114 Tungpradubkul et al 1988 Bt israelensis Cry4Ba3 AAA22337 Yamamoto et al 1988 Bt israelensis Cry4Ba4 BAA00178 Sen et al 1988 Bt israelensis HD522 Cry4Ba5 CAD30095 Berry et al 2002 Bt israelensis Cry4Ba-like ABC47686 Mahalakshmi et al 2005 Bt LDC-9 insufficient sequence Cry4Ca1 EU646202 Shu et al 2008 No NCBI link July 2009 Cry4Cb1 FJ403208 Jun & Furong 2008 Bt HS18-1 No NCBI link July 2009 Cry4Cb2 FJ597622 Jun & Furong 2008 BT Ywc2-8 No NCBI link July 2009 Cry4Cc1 FJ403207 Jun & Furong 2008 Bt MC28 No NCBI link July 2009 Cry5Aa1 AAA67694 Narva et al 1994 Bt darmstadiensis PS17 Cry5Ab1 AAA67693 Narva et al 1991 Bt darmstadiensis PS17 Cry5Ac1 I34543 Payne et al 1997 DNA sequence only Cry5Ad1 ABQ82087 Lenane et al 2007 Bt L366 Cry5Ba1 AAA68598 Foncerrada & Narva 1997 Bt PS86Q3 Cry5Ba2 ABW88931 Guo et al 2008 YBT 1518 Cry6Aa1 AAA22357 Narva et al 1993 Bt PS52A1 Cry6Aa2 AAM46849 Bai et al 2001 YBT 1518 Cry6Aa3 ABH03377 Jia et al 2006 Bt 96418 Cry6Ba1 AAA22358 Narva et al 1991 Bt PS69D1 Cry7Aa1 AAA22351 Lambert et al 1992 Bt galleriae PGSI245 Cry7Ab1 AAA21120 Narva & Fu 1994 Bt dakota HD511 Cry7Ab2 AAA21121 Narva & Fu 1994 Bt kumamotoensis 867 Cry7Ab3 ABX24522 Song et al 2008 Bt WZ-9 Cry7Ab4 EU380678 Shu et al 2008 Bt No NCBI link July 2009 Cry7Ab5 ABX79555 Aguirre-Arzola et al 2008 Bt monterrey GM-33 Cry7Ab6 ACI44005 Deng et al 2008 Bt HQ122 Cry7Ab7 FJ940776 Wang et al 2009 No NCBI link September 2009 Cry7Ab8 GU145299 Feng Jing 2009 No NCBI link November 2009 Cry7Ba1 ABB70817 Zhang et al 2006 Bt huazhongensis Cry7Ca1 ABR67863 Gao et al 2007 Bt BTH-13 Cry7Da1 ACQ99547 Yi et al 2009 Bt LH-2 Cry8Aa1 AAA21117 Narva & Fu 1992 Bt kumamotoensis Cry8Ab1 EU044830 Cheng et al 2007 Bt B-JJX No NCBI link July 2009 Cry8Ba1 AAA21118 Narva & Fu 1993 Bt kumamotoensis Cry8Bb1 CAD57542 Abad et al 2002 Cry8Bc1 CAD57543 Abad et al 2002 Cry8Ca1 AAA21119 Sato et al. 1995 Bt japonensis Buibui Cry8Ca2 AAR98783 Shu et al 2004 Bt HBF-1 Cry8Ca3 EU625349 Du et al 2008 Bt FTL-23 No NCBI link July 2009 Cry8Da1 BAC07226 Asano et al 2002 Bt galleriae Cry8Da2 BD133574 Asano et al 2002 Bt DNA sequence only Cry8Da3 BD133575 Asano et al 2002 Bt DNA sequence only Cry8Db1 BAF93483 Yamaguchi et al 2007 Bt BBT2-5 Cry8Ea1 AAQ73470 Fuping et al 2003 Bt 185 Cry8Ea2 EU047597 Liu et al 2007 Bt B-DLL No NCBI link July 2009 Cry8Fa1 AAT48690 Shu et al 2004 Bt 185 also AAW81032 Cry8Ga1 AAT46073 Shu et al 2004 Bt HBF-18 Cry8Ga2 ABC42043 Yan et al 2008 Bt 145 Cry8Ga3 FJ198072 Xiaodong et al 2008 Bt FCD114 No NCBI link July 2009 Cry8Ha1 EF465532 Fuping et al 2006 Bt 185 No NCBI link July 2009 Cry8Ia1 EU381044 Yan et al 2008 Bt su4 No NCBI link July 2009 Cry8Ja1 EU625348 Du et al 2008 Bt FPT-2 No NCBI link July 2009 Cry8Ka1 FJ422558 Quezado et al 2008 No NCBI link July 2009 Cry8Ka2 ACN87262 Noguera & Ibarra 2009 Bt kenyae Cry8-like FJ770571 Noguera & Ibarra 2009 Bt canadensis DNA sequence only Cry8-like ABS53003 Mangena et al 2007 Bt Cry9Aa1 CAA41122 Shevelev et al 1991 Bt galleriae Cry9Aa2 CAA41425 Gleave et al 1992 Bt DSIR517 Cry9Aa3 GQ249293 Su et al 2009 Bt SC5(D2) No NCBI link July 2009 Cry9Aa4 GQ249294 Su et al 2009 Bt T03C001 No NCBI link July 2009 Cry9Aa like AAQ52376 Baum et al 2003 incomplete sequence Cry9Ba1 CAA52927 Shevelev et al 1993 Bt galleriae Cry9Bb1 AAV28716 Silva-Werneck et al 2004 Bt japonensis Cry9Ca1 CAA85764 Lambert et al 1996 Bt tolworthi Cry9Ca2 AAQ52375 Baum et al 2003 Cry9Da1 BAA19948 Asano 1997 Bt japonensis N141 Cry9Da2 AAB97923 Wasano & Ohba 1998 Bt japonensis Cry9Da3 GQ249295 Su et al 2009 Bt T03B001 No NCBI link July 2009 Cry9Da4 GQ249297 Su et al 2009 Bt T03B001 No NCBI link July 2009 Cry9Db1 AAX78439 Flannagan & Abad 2005 Bt kurstaki DP1019 Cry9Ea1 BAA34908 Midoh & Oyama 1998 Bt aizawai SSK-10 Cry9Ea2 AAO12908 Li et al 2001 Bt B-Hm-16 Cry9Ea3 ABM21765 Lin et al 2006 Bt lyA Cry9Ea4 ACE88267 Zhu et al 2008 Bt ywc5-4 Cry9Ea5 ACF04743 Zhu et al 2008 Bts Cry9Ea6 ACG63872 Liu & Guo 2008 Bt 11 Cry9Ea7 FJ380927 Sun et al 2008 No NCBI link July 2009 Cry9Ea8 GQ249292 Su et al 2009 GQ249292 No NCBI link July 2009 Cry9Eb1 CAC50780 Arnaut et al 2001 Cry9Eb2 GQ249298 Su et al 2009 Bt T03B001 No NCBI link July 2009 Cry9Ec1 AAC63366 Wasano et al 2003 Bt galleriae Cry9Ed1 AAX78440 Flannagan & Abad 2005 Bt kurstaki DP1019 Cry9Ee1 GQ249296 Su et al 2009 Bt T03B001 No NCBI link August 2009 Cry9-like AAC63366 Wasano et al 1998 Bt galleriae insufficient sequence Cry10Aa1 AAA22614 Thorne et al 1986 Bt israelensis Cry10Aa2 E00614 Aran & Toomasu 1996 Bt israelensis ONR-60A DNA sequence only Cry10Aa3 CAD30098 Berry et al 2002 Bt israelensis Cry10A-like DQ167578 Mahalakshmi et al 2006 Bt LDC-9 incomplete sequence Cry11Aa1 AAA22352 Donovan et al 1988 Bt israelensis Cry11Aa2 AAA22611 Adams et al 1989 Bt israelensis Cry11Aa3 CAD30081 Berry et al 2002 Bt israelensis Cry11Aa-like DQ166531 Mahalakshmi et al 2007 Bt LDC-9 incomplete sequence Cry11Ba1 CAA60504 Delecluse et al 1995 Bt jegathesan 367 Cry11Bb1 AAC97162 Orduz et al 1998 Bt medellin Cry12Aa1 AAA22355 Narva et al 1991 Bt PS33F2 Cry13Aa1 AAA22356 Narva et al 1992 Bt PS63B Cry14Aa1 AAA21516 Narva et al 1994 Bt sotto PS80JJ1 Cry15Aa1 AAA22333 Brown & Whiteley 1992 Bt thompsoni Cry16Aa1 CAA63860 Barloy et al 1996 Cb malaysia CH18 Cry17Aa1 CAA67841 Barloy et al 1998 Cb malaysia CH18 Cry18Aa1 CAA67506 Zhang et al 1997 Paenibacillus popilliae Cry18Ba1 AAF89667 Patel et al 1999 Paenibacillus popilliae Cry18Ca1 AAF89668 Patel et al 1999 Paenibacillus popilliae Cry19Aa1 CAA68875 Rosso & Delecluse 1996 Bt jegathesan 367 Cry19Ba1 BAA32397 Hwang et al 1998 Bt higo Cry20Aa1 AAB93476 Lee & Gill 1997 Bt fukuokaensis Cry20Ba1 ACS93601 Noguera & Ibarra 2009 Bt higo LBIT-976 Cry20-like GQ144333 Yi et al 2009 Bt Y-5 DNA sequence only Cry21Aa1 I32932 Payne et al 1996 DNA sequence only Cry21Aa2 I66477 Feitelson 1997 DNA sequence only Cry21Ba1 BAC06484 Sato & Asano 2002 Bt roskildiensis Cry22Aa1 I34547 Payne et al 1997 DNA sequence only Cry22Aa2 CAD43579 Isaac et al 2002 Bt Cry22Aa3 ACD93211 Du et al 2008 Bt FZ-4 Cry22Ab1 AAK50456 Baum et al 2000 Bt EG4140 Cry22Ab2 CAD43577 Isaac et al 2002 Bt Cry22Ba1 CAD43578 Isaac et al 2002 Bt Cry23Aa1 AAF76375 Donovan et al 2000 Bt Binary with Cry37Aa1 Cry24Aa1 AAC61891 Kawalek and Gill 1998 Bt jegathesan Cry24Ba1 BAD32657 Ohgushi et al 2004 Bt sotto Cry24Ca1 CAJ43600 Beron & Salerno 2005 Bt FCC-41 Cry25Aa1 AAC61892 Kawalek and Gill 1998 Bt jegathesan Cry26Aa1 AAD25075 Wojciechowska et al 1999 Bt finitimus B-1166 Cry27Aa1 BAA82796 Saitoh 1999 Bt higo Cry28Aa1 AAD24189 Wojciechowska et al 1999 Bt finitimus B-1161 Cry28Aa2 AAG00235 Moore and Debro 2000 Bt finitimus Cry29Aa1 CAC80985 Delecluse et al 2000 Bt medellin Cry30Aa1 CAC80986 Delecluse et al 2000 Bt medellin Cry30Ba1 BAD00052 Ito et al 2003 Bt entomocidus Cry30Ca1 BAD67157 Ohgushi et al 2004 Bt sotto Cry30Ca2 ACU24781 Sun and Park 2009 Bt jegathesan 367 Cry30Da1 EF095955 Shu et al 2006 Bt Y41 No NCBI link July 2009 Cry30Db1 BAE80088 Kishida et al 2006 Bt aizawai BUN1-14 Cry30Ea1 ACC95445 Fang et al 2007 Bt S2160-1 Cry30Ea2 FJ499389 Jun et al 2008 Bt Ywc2-8 No NCBI link July 2009 Cry30Fa1 ACI22625 Tan et al 2008 Bt MC28 Cry30Ga1 ACG60020 Zhu et al 2008 Bt HS18-1 Cry31Aa1 BAB11757 Saitoh & Mizuki 2000 Bt 84-HS-1-11 Cry31Aa2 AAL87458 Jung and Cote 2000 Bt M15 Cry31Aa3 BAE79808 Uemori et al 2006 Bt B0195 Cry31Aa4 BAF32571 Yasutake et al 2006 Bt 79-25 Cry31Aa5 BAF32572 Yasutake et al 2006 Bt 92-10 Cry31Ab1 BAE79809 Uemori et al 2006 Bt B0195 Cry31Ab2 BAF32570 Yasutake et al 2006 Bt 31-5 Cry31Ac1 BAF34368 Yasutake et al 2006 Bt 87-29 Cry32Aa1 AAG36711 Balasubramanian et al 2001 Bt yunnanensis Cry32Ba1 BAB78601 Takebe et al 2001 Bt Cry32Ca1 BAB78602 Takebe et al 2001 Bt Cry32Da1 BAB78603 Takebe et al 2001 Bt Cry33Aa1 AAL26871 Kim et al 2001 Bt dakota Cry34Aa1 AAG50341 Ellis et al 2001 Bt PS80JJ1 Binary with Cry35Aa1 Cry34Aa2 AAK64560 Rupar et al 2001 Bt EG5899 Binary with Cry35Aa2 Cry34Aa3 AAT29032 Schnepf et al 2004 Bt PS69Q Binary with Cry35Aa3 Cry34Aa4 AAT29030 Schnepf et al 2004 Bt PS185GG Binary with Cry35Aa4 Cry34Ab1 AAG41671 Moellenbeck et al 2001 Bt PS149B1 Binary with Cry35Ab1 Cry34Ac1 AAG50118 Ellis et al 2001 Bt PS167H2 Binary with Cry35Ac1 Cry34Ac2 AAK64562 Rupar et al 2001 Bt EG9444 Binary with Cry35Ab2 Cry34Ac3 AAT29029 Schnepf et al 2004 Bt KR1369 Binary with Cry35Ab3 Cry34Ba1 AAK64565 Rupar et al 2001 Bt EG4851 Binary with Cry35Ba1 Cry34Ba2 AAT29033 Schnepf et al 2004 Bt PS201L3 Binary with Cry35Ba2 Cry34Ba3 AAT29031 Schnepf et al 2004 Bt PS201HH2 Binary with Cry35Ba3 Cry35Aa1 AAG50342 Ellis et al 2001 Bt PS80JJ1 Binary with Cry34Aa1 Cry35Aa2 AAK64561 Rupar et al 2001 Bt EG5899 Binary with Cry34Aa2 Cry35Aa3 AAT29028 Schnepf et al 2004 Bt PS69Q Binary with Cry34Aa3 Cry35Aa4 AAT29025 Schnepf et al 2004 Bt PS185GG Binary with Cry34Aa4 Cry35Ab1 AAG41672 Moellenbeck et al 2001 Bt PS149B1 Binary with Cry34Ab1 Cry35Ab2 AAK64563 Rupar et al 2001 Bt EG9444 Binary with Cry34Ac2 Cry35Ab3 AY536891 AAT29024 2004 Bt KR1369 Binary with Cry34Ab3 Cry35Ac1 AAG50117 Ellis et al 2001 Bt PS167H2 Binary with Cry34Ac1 Cry35Ba1 AAK64566 Rupar et al 2001 Bt EG4851 Binary with Cry34Ba1 Cry35Ba2 AAT29027 Schnepf et al 2004 Bt PS201L3 Binary with Cry34Ba2 Cry35Ba3 AAT29026 Schnepf et al 2004 Bt PS201HH2 Binary with Cry34Ba3 Cry36Aa1 AAK64558 Rupar et al 2001 Bt Cry37Aa1 AAF76376 Donovan et al 2000 Bt Binary with Cry23Aa Cry38Aa1 AAK64559 Rupar et al 2000 Bt Cry39Aa1 BAB72016 Ito et al 2001 Bt aizawai Cry40Aa1 BAB72018 Ito et al 2001 Bt aizawai Cry40Ba1 BAC77648 Ito et al 2003 Bun1-14 Cry40Ca1 EU381045 Shu et al 2008 Bt Y41 No NCBI link July 2009 Cry40Da1 ACF15199 Zhang et al 2008 Bt S2096-2 Cry41Aa1 BAD35157 Yamashita et al 2003 Bt A1462 Cry41Ab1 BAD35163 Yamashita et al 2003 Bt A1462 Cry42Aa1 BAD35166 Yamashita et al 2003 Bt A1462 Cry43Aa1 BAD15301 Yokoyama and Tanaka 2003 P. lentimorbus semadara Cry43Aa2 BAD95474 Nozawa 2004 P. popilliae popilliae Cry43Ba1 BAD15303 Yokoyama and Tanaka 2003 P. lentimorbus semadara Cry43-like BAD15305 Yokoyama and Tanaka 2003 P. lentimorbus semadara Cry44Aa BAD08532 Ito et al 2004 Bt entomocidus INA288 Cry45Aa BAD22577 Okumura et al 2004 Bt 89-T-34-22 Cry46Aa BAC79010 Ito et al 2004 Bt dakota Cry46Aa2 BAG68906 Ishikawa et al 2008 Bt A1470 Cry46Ab BAD35170 Yamagiwa et al 2004 Bt Cry47Aa AAY24695 Kongsuwan et al 2005 Bt CAA890 Cry48Aa CAJ18351 Jones and Berry 2005 Bs IAB59 binary with 49Aa Cry48Aa2 CAJ86545 Jones and Berry 2006 Bs 47-6B binary with 49Aa2 Cry48Aa3 CAJ86546 Jones and Berry 2006 Bs NHA15b binary with 49Aa3 Cry48Ab CAJ86548 Jones and Berry 2006 Bs LP1G binary with 49Ab1 Cry48Ab2 CAJ86549 Jones and Berry 2006 Bs 2173 binary with 49Aa4 Cry49Aa CAH56541 Jones and Berry 2005 Bs IAB59 binary with 48Aa Cry49Aa2 CAJ86541 Jones and Berry 2006 Bs 47-6B binary with 48Aa2 Cry49Aa3 CAJ86543 Jones and Berry 2006 BsNHA15b binary with 48Aa3 Cry49Aa4 CAJ86544 Jones and Berry 2006 Bs 2173 binary with 48Ab2 Cry49Ab1 CAJ86542 Jones and Berry 2006 Bs LP1G binary with 48Ab1 Cry50Aa1 BAE86999 Ohgushi et al 2006 Bt sotto Cry51Aa1 ABI14444 Meng et al 2006 Bt F14-1 Cry52Aa1 EF613489 Song et al 2007 Bt Y41 No NCBI link July 2009 Cry52Ba1 FJ361760 Jun et al 2008 Bt BM59-2 No NCBI link July 2009 Cry53Aa1 EF633476 Song et al 2007 Bt Y41 No NCBI link July 2009 Cry53Ab1 FJ361759 Jun et al 2008 Bt MC28 No NCBI link July 2009 Cry54Aa1 ACA52194 Tan et al 2009 Bt MC28 Cry55Aa1 ABW88932 Guo et al 2008 YBT 1518 Cry55Aa2 AAE33526 Bradfisch et al 2000 BT Y41 Cry56Aa1 FJ597621 Jun & Furong 2008 Bt Ywc2-8 No NCBI link July 2009 Cry56Aa2 GQ483512 Guan Peng et al 2009 Bt G7-1 No NCBI link August 2009 Cry57Aa1 ANC87261 Noguera & Ibarra 2009 Bt kim Cry58Aa1 ANC87260 Noguera & Ibarra 2009 Bt entomocidus Cry59Aa1 ACR43758 Noguera & Ibarra 2009 Bt kim LBIT-980 Vip3Aa1 Vip3Aa AAC37036 Estruch et al 1996 PNAS 93, AB88 5389-5394 Vip3Aa2 Vip3Ab AAC37037 Estruch et al 1996 PNAS 93, AB424 5389-5394 Vip3Aa3 Vip3Ac Estruch et al 2000 U.S. Pat. No. 6,137,033 October 2000 Vip3Aa4 PS36A Sup AAR81079 Feitelson et al 1998 U.S. Pat. No. Bt PS36A WO9818932(A2, A3) 6,656,908 7 May 1998 December 2003 Vip3Aa5 PS81F Sup AAR81080 Feitelson et al 1998 U.S. Pat. No. Bt PS81F WO9818932(A2, A3) 6,656,908 7 May 1998 December 2003 Vip3Aa6 Jav90 Sup AAR81081 Feitelson et al 1998 U.S. Pat. No. Bt WO9818932(A2, A3) 6,656,908 7 May 1998 December 2003 Vip3Aa7 Vip83 AAK95326 Cai et al 2001 unpublished Bt YBT-833 Vip3Aa8 Vip3A AAK97481 Loguercio et al 2001 unpublished Bt HD125 Vip3Aa9 VipS CAA76665 Selvapandiyan 2001 unpublished Bt A13 et al Vip3Aa10 Vip3V AAN60738 Doss et al 2002 Protein Expr. Bt Purif. 26, 82-88 Vip3Aa11 Vip3A AAR36859 Liu et al 2003 unpublished Bt C9 Vip3Aa12 Vip3A-WB5 AAM22456 Wu and Guan 2003 unpublished Bt Vip3Aa13 Vip3A AAL69542 Chen et al 2002 Sheng Wu Bt S184 Gong Cheng Xue Bao 18, 687-692 Vip3Aa14 Vip AAQ12340 Polumetla et al 2003 unpublished Bt tolworthi Vip3Aa15 Vip3A AAP51131 Wu et al 2004 unpublished Bt WB50 Vip3Aa16 Vip3LB AAW65132 Mesrati et al 2005 FEMS Micro Bt Lett 244, 353-358 Vip3Aa17 Jav90 Feitelson et al 1999 U.S. Pat. No. Javelin 1990 WO9957282(A2, A3) 6,603,063 11 Nov. 1999 August 2003 Vip3Aa18 AAX49395 Cai and Xiao 2005 unpublished Bt 9816C Vip3Aa19 Vip3ALD DQ241674 Liu et al 2006 unpublished Bt AL Vip3Aa19 Vip3A-1 DQ539887 Hart et al 2006 unpublished Vip3Aa20 Vip3A-2 DQ539888 Hart et al 2006 unpublished Vip3Aa21 Vip ABD84410 Panbangred 2006 unpublished Bt aizawai Vip3Aa22 Vip3A-LS1 AAY41427 Lu et al 2005 unpublished Bt LS1 Vip3Aa23 Vip3A-LS8 AAY41428 Lu et al 2005 unpublished Bt LS8 Vip3Aa24 BI 880913 Song et al 2007 unpublished Bt WZ-7 Vip3Aa25 EF608501 Hsieh et al 2007 unpublished Vip3Aa26 EU294496 Shen and Guo 2007 unpublished Bt TF9 Vip3Aa27 EU332167 Shen and Guo 2007 unpublished Bt 16 Vip3Aa28 FJ494817 Xiumei Yu 2008 unpublished Bt JF23-8 Vip3Aa29 FJ626674 Xieumei et al 2009 unpublished Bt JF21-1 Vip3Aa30 FJ626675 Xieumei et al 2009 unpublished MD2-1 Vip3Aa31 FJ626676 Xieumei et al 2009 unpublished JF21-1 Vip3Aa32 FJ626677 Xieumei et al 2009 unpublished MD2-1 . . Vip3Ab1 Vip3B AAR40284 Feitelson et al 1999 U.S. Pat. No. Bt KB59A4-6 WO9957282(A2, A3) 6,603,063 11 Nov. 1999 August 2003 Vip3Ab2 Vip3D AAY88247 Feng and Shen 2006 unpublished Bt . . Vip3Ac1 PS49C Narva et al . US application 20040128716 . . Vip3Ad1 PS158C2 Narva et al . US application 20040128716 Vip3Ad2 ISP3B CAI43276 Van Rie et al 2005 unpublished Bt . . Vip3Ae1 ISP3C CAI43277 Van Rie et al 2005 unpublished Bt . . Vip3Af1 ISP3A CAI43275 Van Rie et al 2005 unpublished Bt Vip3Af2 Vip3C ADN08753 Syngenta . WO 03/075655 . . Vip3Ag1 Vip3B ADN08758 Syngenta . WO 02/078437 Vip3Ag2 FJ556803 Audtho et al 2008 Bt . . Vip3Ah1 Vip3S DQ832323 Li and Shen 2006 unpublished Bt . Vip3Ba1 AAV70653 Rang et al 2004 unpublished . Vip3Bb1 Vip3Z ADN08760 Syngenta . WO 03/075655 Vip3Bb2 EF439819 Akhurst et al 2007 

We claim:
 1. A transgenic plant comprising DNA encoding a Cry1Be insecticidal protein and DNA encoding a Cry1Fa insecticidal protein, wherein said Cry1Fa insecticidal protein is at least 95% identical with SEQ ID NO:1, and said Cry1Be insecticidal protein is at least 95% identical with SEQ ID NO:2, wherein said transgenic plant expresses an effective amount of said Cry1Fa insecticidal protein and said Cry1Be insecticidal protein to prevent development of Cry-resistant lepidopteran pests, and wherein said Cry1Fa insecticidal protein and said Cry1Be insecticidal protein do not share a receptor binding site in European corn borer (ECB) gut and do not share a receptor binding site in fall armyworm (FAW) gut.
 2. A seed of the plant of claim 1 comprising DNA encoding said Cry1Be insecticidal protein and DNA encoding said Cry1Fa insecticidal protein.
 3. A plurality of plants comprising non-Bt refuge plants and a plurality of transgenic plants of claim 1, wherein said refuge plants comprise less than 40% of all crop plants in said plurality of plants.
 4. The plurality of plants of claim 3, wherein said refuge plants are in blocks or strips.
 5. A mixture of seeds comprising refuge seeds from non-Bt refuge plants, and a plurality of seeds of claim 2, wherein said refuge seeds comprise less than 40% of all the seeds in the mixture.
 6. A method of managing development of resistance to a Cry toxin by an insect, said method comprising planting seeds to produce the plurality of plants of claim
 3. 7. A composition for controlling Cry1Fa-resistant lepidopteran pests, said composition comprising cells that express effective amounts of both a Cry1Fa core toxin-containing protein and a Cry1Be core toxin-containing protein, wherein said Cry1Fa core-toxin containing protein and said Cry1Be core toxin-containing insecticidal protein do not share a receptor binding site in ECB gut and do not share a receptor binding site in FAW gut.
 8. The composition of claim 7 comprising a host transformed to express both said Cry1Fa protein and said Cry1Be protein, wherein said host is a microorganism or a plant cell.
 9. A method of controlling Cry1Fa-resistant lepidopteran pests, said method comprising presenting to said pests or to the environment of said pests an effective amount of the composition of claim 7, wherein said lepidopteran pests are selected from the group consisting of European corn borer and fall armyworm.
 10. A transgenic plant that produces four insecticidal proteins derived from Bacillus thuringiensis, wherein three of said proteins provide non-cross-resistant activity against a first insect, and three of said proteins provide non-cross-resistant activity against a second insect, wherein said plant comprises DNA encoding a Cry1Fa insecticidal protein and DNA encoding a Cry1Be insecticidal protein, wherein said first insect is European corn borer and said second insect is fall armyworm, and wherein said Cry1Fa insecticidal protein and said Cry1Be insecticidal protein do not share a receptor binding site in ECB gut and do not share a receptor binding site in FAW gut.
 11. The transgenic plant of claim 1, wherein the plant produces a third protein selected from the group consisting of Cry1Ab, Cry2Aa, and Cry1I proteins.
 12. The transgenic plant of claim 1, wherein the plant produces a third protein selected from the group consisting of Vip3A, Cry1C, Cry1D, and Cry1E proteins.
 13. The transgenic plant of claim 11, wherein the plant produces a fourth protein selected from the group consisting of Vip3A, Cry1C, Cry1D, and Cry1E proteins.
 14. A method of managing development of resistance to a Cry1Fa toxin by European corn borer and fall armyworm, said method comprising planting seeds to produce the transgenic plant of claim
 10. 15. A plurality of plants comprising non-Bt refuge plants and a plurality of the transgenic plants of claim 10, wherein said refuge plants comprise less than about 20% of all crop plants in said plurality of plants.
 16. A method of managing development of resistance to a Cry1Fa toxin by European corn borer and fall armyworm, said method comprising planting seeds to produce the plurality of plants of claim
 15. 17. A mixture of seeds comprising refuge seeds from non-Bt refuge plants, and a plurality of transgenic seeds from the plant of claim 10, wherein said refuge seeds comprise less than 10% of all the seeds in the mixture.
 18. A plant cell of the plant of claim 1, wherein said plant cell comprises said DNA encoding said Cry1Fa insecticidal protein and said DNA encoding said Cry1Be insecticidal protein, wherein said Cry1Fa insecticidal protein is at least 99% identical with SEQ ID NO: 1, and said Cry1Be insecticidal protein is at least 99% identical with SEQ ID NO:
 2. 19. The plant of claim 1, wherein said Cry1Fa insecticidal protein comprises SEQ ID NO:1, and said Cry1Be insecticidal protein comprises SEQ ID NO:2.
 20. A method of controlling a Cry resistant insect selected from the group consisting of a European corn borer and a fall armyworm, said method comprising contacting said insect with a Cry1Be insecticidal protein and a Cry1Fa insecticidal protein, wherein said Cry1Fa insecticidal protein and said Cry1Be insecticidal protein do not share a receptor binding site in ECB gut and do not share a receptor binding site in FAW gut.
 21. A plant cell of the plant of claim 10, wherein said Cry1Fa insecticidal protein is at least 99% identical with SEQ ID NO:1, and said Cry1Be insecticidal protein is at least 99% identical with SEQ ID NO:2.
 22. The plant of claim 10, wherein said Cry1Fa insecticidal protein comprises SEQ ID NO:1, and said Cry1Be insecticidal protein comprises SEQ ID NO:2. 